Catalyst Life Sciences is currently partnered with a large and fast growing pharma company for their Houston, TX facility. Ideal candidates should be coming from a project management background with a proven record of customer service optimization.
Day to day you will:
To be successful you should have:
We are working with a leading compounding pharmacy to find a Supervisor/Shift Manager for the Aseptic Filling department and ensure high-quality, safe, and efficient production processes. This role involves overseeing aseptic filling operations, ensuring compliance with GMP and FDA standards, and driving continuous improvement strategies.
Required Experience:
Our client is actively looking for a Sr Manager of Facilities and Maintenance. This is an on-site position based in East Windsor NJ.
You should apply if you have:
Our client is actively looking for a Validation Manager. This is an on-site position in the Cranbury NJ area.
We’re Hiring: Senior Chemist Location: Clifton NJ
Our client is seeking a Senior Chemist to join their dynamic Quality team. The ideal candidate will play a critical role in ensuring the integrity and compliance of their high-quality products.
Key Requirements:
Expert-level proficiency in HPLC (High-Performance Liquid Chromatography) and NCC (Nutritional Composition Compliance)
Proven experience in product release within nutraceutical or dietary supplement companies
Strong analytical skills, attention to detail, and a commitment to quality standards
Location: Plymouth, MN Employment Type: Contract to Hire
We are seeking a Design Assurance Engineer with a background in mechanical or biomedical engineering to join our dynamic, fast-paced team. This role will help ensure compliance with our internal SOPs and product lifecycle processes, and play a key part in preparing the organization for ISO 13485 certification and FDA audits.
Ensure adherence to company’s APDP (Advanced Product Development Process) lifecycle SOPs (Phase 0–3).
Monitor and enforce compliance with design control and quality guidance documents.
Support audit readiness for FDA inspections and ISO 13485 certification.
Collaborate with R&D to ensure documentation and processes align with regulatory expectations.
Bring technical understanding to design reviews, supporting risk management and design inputs/outputs.
Help optimize project plans and timelines without compromising compliance.
Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field.
Minimum 3–5 years of experience in design assurance or quality engineering in the medical device industry.
Strong understanding of ISO 13485 and FDA regulations.
Technical aptitude – ability to understand and discuss mechanical engineering principles
Excellent organizational skills and attention to detail.
Prior experience in a startup or dynamic development environment is a plus.
Catalyst is seeking to identify a Formulations Director for a rapidly growing life sciences organization. In this role you’d be leading the formulations team in developing new products.
This is an on-site position in Houston, TX.
The position requires the following experience:
Our client is actively looking for a Senior Director of Quality Operations. This is an on-site position in Houston TX.
We’re looking for a Brand Medical Lead with Acute Lymphoblastic Leukemia expertise to join a leading big pharma company! In this role, you’ll work cross-functionally with key internal players, especially Clinical Development and Clinical Operations, to support an early-stage pipeline asset in the ALL disease state.
The right candidate will have:
Our client is actively looking for a Senior Director of Quality Control. This is an on-site position in Cranbury NJ.
